000 00960cam a2200325 4500
001 PUB10999
008 090401t2001 xxu||||| |||| 00| 0 eng d
035 _aPUB10999
037 _bMBI
099 _a11873
100 1 0 _aHunt, D. M.
222 _aEuropean Journal of Human Genetics
245 1 0 _aSpectrum of dominant mutations in the desmosomal cadherin desmoglein 1, causing the skin disease striate palmoplantar keratoderma
700 1 0 _aArmstrong, D. K. B.
700 1 0 _aArnemann, J.
700 1 0 _aBuxton, R. S.
700 1 0 _aDopping-Hepenstal, P. J. C.
700 1 0 _aEady, R. A.
700 1 0 _aHennies, H. C.
700 1 0 _aHughes, A. E.
700 1 0 _aKelsell, D. P.
700 1 0 _aKuster, W.
700 1 0 _aLeigh, I. M.
700 1 0 _aMcGrath, J. A.
700 1 0 _aRickman, L.
700 1 0 _aSimrak, D.
700 1 0 _aStevens, H. P.
_93533
700 1 0 _aWhittock, N. V.
773 _tEuropean Journal of Human Genetics
_g9 (3), 197-203.
999 _c59726
_d59726